A novel strategy for N-alkylation of primary amines+

Article abstract of DOI:10.1080/00397919908086201

N-alkylation of primary amines has been carried out with alkylbromide using commercial Me₂SO and K₂CO₃ as a base. This process offers a method of selection for obtaining either mono or dialkyl amines.

Full text of DOI:10.1080/00397919908086201

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Synthetic Communications: An
International Journal for Rapid
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Organic Chemistry
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A Novel Strategy for N-
Alkylation of Primary Amines
a
a
Sanjay K. Srivastava , Prem Man Singh Chauhan &
a
Amiya P. Bhaduri
a
Division of Medicinal Chemistry, Central Drug
Research Institute, Lucknow, 226001, India
Available online: 17 Sep 2007
To cite this article: Sanjay K. Srivastava, Prem Man Singh Chauhan & Amiya P.
Bhaduri (1999): A Novel Strategy for N-Alkylation of Primary Amines, Synthetic
Communications: An International Journal for Rapid Communication of Synthetic
Organic Chemistry, 29:12, 2085-2091
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